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Trial · NCT04283669

Phase 2 Clinical Trial of Crizotinib for Children and Adults With Neurofibromatosis Type 2 and Progressive Vestibular Schwannomas

NCT04283669, Phase 2, Completed, University of Alabama at Birmingham; results first posted 2026-03-13

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Phase 2 Clinical Trial of Crizotinib for Children and Adults With Neurofibromatosis Type 2 and Progressive Vestibular Schwannomas. Trials, record NCT04283669. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04283669

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Phase 2 Clinical Trial of Crizotinib for Children and Adults With Neurofibromatosis Type 2 and Progressive Vestibular Schwannomas
NCT number
NCT04283669
Status
Completed
Phases
Phase 2
Enrollment
12 participants, actual
Lead sponsor
University of Alabama at Birmingham
Conditions
Neurofibromatosis 2, Progressive Vestibular Schwannoma (VS)
Interventions
Crizotinib
First posted
2020-02-25
Last updated
2026-03-13
Results first posted
2026-03-13

Source ClinicalTrials.gov

Registered outcomes1

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryVolumetric Response RateUp to 48 Weeks
To evaluate efficacy, imaging response is treated as a binary variable whereby patients who achieve a volumetric response (greater than 20% reduction in tumor volume) in the target tumor at any point within 12 months from beginning of therapy are considered responders and all other patients are nonresponders.

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYVolumetric Response RateUp to 48 WeeksAnalysis population consists of 9 participants that received the study treatment.ParticipantsCOUNT_OF_PARTICIPANTS

Results by group2

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Volumetric Response RateOpen Label Continuous TreatmentResponders0Participants
Volumetric Response RateOpen Label Continuous TreatmentNon-responders9Participants

Participant flow3

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDOpen Label Continuous Treatment9
Overall StudyCOMPLETEDOpen Label Continuous Treatment4
Overall StudyNOT COMPLETEDOpen Label Continuous Treatment5

Adverse events43

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAnemiaBlood and lymphatic system disordersOpen Label Continuous Treatment19
otherTinnitusEar and labyrinth disordersOpen Label Continuous Treatment29
otherBlurred visionEye disordersOpen Label Continuous Treatment19
otherExtraocular muscle paresisEye disordersOpen Label Continuous Treatment19
otherEye Disorders - Other, Astrocytic Retinal HamartomasEye disordersOpen Label Continuous Treatment19
otherEye Disorders - Other, Shutter Like EffectEye disordersOpen Label Continuous Treatment19
otherEye Disorders - Other, Vision ChangesEye disordersOpen Label Continuous Treatment19
otherConstipationGastrointestinal disordersOpen Label Continuous Treatment19
otherDiarrheaGastrointestinal disordersOpen Label Continuous Treatment79
otherDyspepsiaGastrointestinal disordersOpen Label Continuous Treatment39

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityOpen Label Continuous Treatment09
Total, other adverse eventsOpen Label Continuous Treatment99
Total, serious adverse eventsOpen Label Continuous Treatment09

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT04283669

GET https://conductscience.org/api/trials/v1/NCT04283669/events?page=2